Last synced on 18 April 2025 at 11:05 pm

Symbia Pro.specta Q3 (11364751); Symbia Pro.specta X3 (11364752); Symbia Pro.specta X7 (11364753); Symbia Pro.specta VA30A Family

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243186
510(k) Type
Special
Applicant
Siemens Medical Solutions USA, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/2024
Days to Decision
30 days
Submission Type
Summary

Symbia Pro.specta Q3 (11364751); Symbia Pro.specta X3 (11364752); Symbia Pro.specta X7 (11364753); Symbia Pro.specta VA30A Family

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243186
510(k) Type
Special
Applicant
Siemens Medical Solutions USA, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/2024
Days to Decision
30 days
Submission Type
Summary